Baumgartner Adolf, Weier Jingly Fung, Weier Heinz-Ulrich G
Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco, California, CA 94720, USA.
J Histochem Cytochem. 2006 Dec;54(12):1363-70. doi: 10.1369/jhc.6A6974.2006. Epub 2006 Aug 21.
In research as well as in clinical applications, fluorescence in situ hybridization (FISH) has gained increasing popularity as a highly sensitive technique to study cytogenetic changes. Today, hundreds of commercially available DNA probes serve the basic needs of the biomedical research community. Widespread applications, however, are often limited by the lack of appropriately labeled, specific nucleic acid probes. We describe two approaches for an expeditious preparation of chromosome-specific DNAs and the subsequent probe labeling with reporter molecules of choice. The described techniques allow the preparation of highly specific DNA repeat probes suitable for enumeration of chromosomes in interphase cell nuclei or tissue sections. In addition, there is no need for chromosome enrichment by flow cytometry and sorting or molecular cloning. Our PCR-based method uses either bacterial artificial chromosomes or human genomic DNA as templates with alpha-satellite-specific primers. Here we demonstrate the production of fluorochrome-labeled DNA repeat probes specific for human chromosomes 17 and 18 in just a few days without the need for highly specialized equipment and without the limitation to only a few fluorochrome labels.
在研究以及临床应用中,荧光原位杂交(FISH)作为一种研究细胞遗传学变化的高灵敏度技术越来越受欢迎。如今,数百种市售的DNA探针满足了生物医学研究界的基本需求。然而,广泛的应用常常受到缺乏适当标记的特异性核酸探针的限制。我们描述了两种快速制备染色体特异性DNA以及随后用所选报告分子进行探针标记的方法。所描述的技术允许制备适用于对间期细胞核或组织切片中的染色体进行计数的高度特异性DNA重复探针。此外,无需通过流式细胞术和分选或分子克隆进行染色体富集。我们基于PCR的方法使用细菌人工染色体或人类基因组DNA作为模板,以及α卫星特异性引物。在这里,我们展示了仅需几天时间就能生产出针对人类17号和18号染色体的荧光染料标记的DNA重复探针,无需高度专业化的设备,也不受限于仅几种荧光染料标记。